MIR3915 microRNA 3915

Information
Symbol
MIR3915
Type
ncRNA
Description
microRNA 3915
Entrez Gene ID
100500915
Genome
hg19
Position
chrX:32,601,773-32,601,869
Genome
hg38
Position
chrX:32,583,656-32,583,752
HGNC
HGNC:38955 HGNC
Ensembl
ENSG00000263600 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 7 0
Ranking
ClinVar
0
0
0
0
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
HGNC HGNC:38955 HGNC
Ensembl ENSG00000263600 Ensembl
miRBase MI0016420
AllianceGenome HGNC:38955
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000578518.1 hg38 chrX 32,583,656 32,583,752 97
ENST00000578518.1 hg19 chrX 32,601,773 32,601,869 97
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